K-number	K102072
Device name	MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)
Applicant	Memometal Technologies
Product code	HTY
Device class	Class II
Decision date	Nov 3, 2010
Decision	Substantially Equivalent
Regulation	888.3040

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View the full FDA submission: accessdata.fda.gov

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MEMOMETAL IMPLANTS (K-SNAP & TI-FUSE)

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